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http://dx.doi.org/10.25259/IJDVL_799_2024DOI Listing

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Article Synopsis
  • Deucravacitinib, an oral tyrosine kinase 2 inhibitor, is approved globally for treating adults with moderate to severe plaque psoriasis, especially those needing systemic therapy.
  • A systematic review and meta-analysis analyzed its efficacy in Asian populations compared to other treatments, revealing significant improvement over placebo and apremilast.
  • In Asian patients, deucravacitinib showed PASI 75 and 90 response rates that are comparable to several biologics, highlighting its effectiveness and convenience as an oral treatment option.
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Objectives: Oligoarticular psoriatic arthritis (PsA) is frequent but rarely studied. The objective was to assess the efficacy of apremilast in early oligoarticular PsA.

Methods: FOREMOST (NCT03747939) was a phase 4 multicentre, randomised, double-blind, placebo-controlled trial.

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Introduction: Deucravacitinib, a novel, oral, selective allosteric tyrosine kinase 2 inhibitor, demonstrated superiority versus placebo and apremilast in the POETYK PSO-1 and PSO-2 studies. We describe patient-reported outcomes with deucravacitinib treatment versus placebo and apremilast in these studies.

Methods: Two multicenter, global, double-blind, placebo- and active comparator-controlled studies randomized patients with moderate-to-severe plaque psoriasis 1:2:1 to placebo, deucravacitinib 6 mg once daily, or apremilast 30 mg twice daily.

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